Canonical Allele Identifier: CA1929213761

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762774C= , CM000672.2:g.94762774C=	GRCh38
NC_000010.10:g.96522531C= , CM000672.1:g.96522531C=	GRCh37
NC_000010.9:g.96512521C=	NCBI36
NG_008384.2:g.5069C=
NG_008384.3:g.5094C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.69C= MANE Select	ENSP00000360372.3:p.Ser23=
ENST00000371321.7:c.69C=	ENSP00000360372.3:p.Ser23=
ENST00000464755.1:c.932-12284C=	ENSP00000483243.1:n.932-12284C=
ENST00000480405.2:c.69C=	ENSP00000483847.1:p.Ser23=
NM_000769.2:c.69C=	NP_000760.1:p.Ser23=
NM_000769.4:c.69C= MANE Select	NP_000760.1:p.Ser23=